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16 The <strong>University</strong> <strong>of</strong> <strong>Kansas</strong> Paleontological Contributions-Paper 99<br />

ington & Clark, 1971; Garden City Limestone,<br />

Wasatch Range; Mason, 1975),<br />

Oklahoma (upper Signal Mountain Limestone,<br />

Wichita Mountains), Texas (uppermost<br />

San Saba Member <strong>of</strong> Wilberns Formation and<br />

lower Threadgill Member <strong>of</strong> Tanyard Formation,<br />

Llano uplift), Pennsylvania-Maryland<br />

(upper Stoufferstown Member <strong>of</strong> Stonehenge<br />

Formation; Tipnis & Goodwin, 1972), and<br />

Wyoming-Montana (Lower Ordovician <strong>of</strong><br />

Bighorn Mountains; Kurtz, 1978). Elsewhere,<br />

C. angulatus is known from northwestern<br />

Greenland (Stouge, 1977), Scandinavia (Lindstrom,<br />

1955; Van Wamel, 1974), Soviet Union<br />

(Viira, 1974), Australia (Druce & Jones, 1971;<br />

Jones, 1971), and Iran (Müller, 1973). In<br />

North America the species is found in Fauna B<br />

(except lowermost part) and lower Fauna C <strong>of</strong><br />

Ethington and Clark (1971). LindstrOm (1955,<br />

pl. 9) recorded C. angulatus through the upper<br />

Tremadocian and into the lower Arenigian<br />

<strong>of</strong> Scandinavia.<br />

CORDYLODUS DRUCEI, new species<br />

Figure 4K, M; Plate 1, figures 177, 20, 21, 25<br />

Cordylodus angulatus Druce and Jones (part),<br />

1971, p. 66, pl. 3, fig. 7 (not figs. 4-6).<br />

Cordylodus cf. C. intermedius Abaimova<br />

(part), 1975, text-fig. 8.42 (not 8.34), pl.<br />

10, fig. 10.<br />

(In part) Cordylodus oklahotnensis Druce and<br />

Jones, 1971, p. 69, text-fig. 23j, pl. 5, figs.<br />

6, 7; ?Jones, 1971, p. 47, pl. 2, figs. 5-8.<br />

(In part) Cordylodus prion Druce and Jones,<br />

1971, p. 70, text-figs. 23i, k-o, pl. 2, figs.<br />

1 -7; not LindstrOm, 1955, p. 552, pl. 2,<br />

figs. 14-16; not Müller, 1973, p. 33, textfig.<br />

2E, 8, pl. 10, fig. 4; not Van Wamel,<br />

1974, p. 59, pl. 1, figs. 8-9; not Viira,<br />

1974, p. 63, pl. 1, figs. 6, 7.<br />

not Cyrtoniodus prion Ethington and Clark,<br />

1971, pl. 1, fig. 21; Miller, 1971, p. 79, pl.<br />

1, figs. 14-17.<br />

Holotype. -Rounded element, USNM<br />

303283 (Fig. 4k; Pl. 1, figs. 20, 21).<br />

Description. -Relatively rare species with<br />

distinctive rounded element and somewhat<br />

variable compressed element. Rounded element<br />

asymmetrical with bulge (caria) on one<br />

side <strong>of</strong> base beneath anterior end <strong>of</strong> denticulate<br />

process; axis <strong>of</strong> bulge trending posteriorly<br />

and downward. Cusp and denticles with<br />

rounded edges; denticles separated at bases.<br />

Basal cavity relatively shallow with apex extending<br />

slightly above top <strong>of</strong> posterior process,<br />

anterior edge concave or straight, apex<br />

not recurved. Anterobasal corner a sharp<br />

angle in primitive elements, but somewhat<br />

rounded in more advanced elements.<br />

Compressed elements less distinctive, may<br />

include two forms. More distinctive form<br />

asymmetrical due to lateral bending and to<br />

presence <strong>of</strong> bulge (caria) on inner side <strong>of</strong><br />

base. Distinctive basal cavity curving concavely<br />

on anterior edge, then bending sharply<br />

near anterobasal corner and subparallel to<br />

basal margin. Basal cavity moderately deep,<br />

apex usually at least as high as top <strong>of</strong> posterior<br />

process but may be shallower in advanced<br />

elements. Second form symmetrical or nearly<br />

so; cusp may be bent slightly to one side and<br />

slight bulge (caria) may exist on inner side<br />

near basal margin. Anterior edge <strong>of</strong> basal<br />

cavity usually convexly curved and extending<br />

about to top <strong>of</strong> posterior process. Both types<br />

<strong>of</strong> compressed elements have laterally compressed<br />

cusps and denticles with sharp edges;<br />

denticles fused at bases.<br />

Discussion. -Two rounded elements, one<br />

illustrated by Druce and Jones (1971, pl. 3,<br />

fig. 7) as C. angulatus and one illustrated by<br />

Abaimova (1975, text-fig. 8.42, pl. 10, fig. 10)<br />

as C. intermedius, have the distinctive characteristics<br />

<strong>of</strong> the rounded element <strong>of</strong> C. drucei,<br />

and they are here reassigned to this new<br />

species.<br />

The rounded element <strong>of</strong> C. drucei is<br />

necessary to permit recognition <strong>of</strong> this species<br />

because <strong>of</strong> the variability <strong>of</strong> the compressed<br />

elements and their similarity to those <strong>of</strong> other<br />

coeval species <strong>of</strong> Cordylodus. The asymmetrical<br />

form is similar to the compressed element<br />

<strong>of</strong> C. intermedius, and the symmetrical form<br />

is similar to the compressed elements <strong>of</strong> C. angulatus<br />

and C. rotundatus. The conclusion<br />

that both types <strong>of</strong> compressed elements were<br />

associated with the distinctive rounded element<br />

<strong>of</strong> C. drucei is uncertain and is based on<br />

the occurrence together <strong>of</strong> all three elements in<br />

many samples.<br />

Cordylodus drucei has three distinguishing<br />

characteristics: a concave anterior edge <strong>of</strong> the

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